Different copy numbers of apparently identically deleted mitochondrial DNA in tissues from a patient with Kearns-Sayre syndrome detected by PCR
- 1 June 1990
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 169 (3) , 1007-1015
- https://doi.org/10.1016/0006-291x(90)91994-4
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Multiple populations of deleted mitochondrial DNA detected by a novel gene amplification methodBiochemical and Biophysical Research Communications, 1989
- Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre SyndromeNew England Journal of Medicine, 1989
- Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndromeNucleic Acids Research, 1989
- Deletions of mitochondrial DNA in Kearns‐Sayre syndromeNeurology, 1988
- Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathyBiochemical and Biophysical Research Communications, 1988
- DELETIONS OF MUSCLE MITOCHONDRIAL DNAThe Lancet, 1988
- KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETIONThe Lancet, 1988
- Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesNature, 1988
- Rapid examination of muscle tissueNeurology, 1963
- Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart BlockA.M.A. Archives of Ophthalmology, 1958